@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_head
{
this:
np:hasAssertion
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion
;
np:hasProvenance
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance
;
np:hasPublicationInfo
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion
a
np:Assertion
.
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance
a
np:Provenance
.
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNef387e92190393580caa8df9905ddf4e
sio:SIO_000628
miriam-gene:79017
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance
{
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion
dcterms:description
"[Several reports have suggested that one or both of the trinucleotide repeat polymorphisms in the human androgen receptor (hAR) gene, (CAG)n coding for polyglutamine and (GGC)n coding for polyglycine, may be associated with prostate cancer risk; but no study has investigated their association with disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:10502720
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}